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Tert-Butyl 3-hydroxy-3-Methylpyrrolidine-1-carboxylate is a chemical compound with the molecular formula C10H19NO3, indicating that it comprises carbon, hydrogen, nitrogen, and oxygen atoms. Its precise molecular structure consists of a pyrrolidine ring, which is a five-membered ring with one nitrogen atom, substituted with a tert-butyl ester and a 3-hydroxy-3-methyl group. Commonly used in various scientific and chemical research, this substance is typically a synthetic intermediate in the manufacture of more complex compounds. It is a colorless or slightly yellow liquid at room temperature, with specific physical and chemical properties, such as boiling point, melting point, and flash point, that may vary based on purity and specific methods and conditions of synthesis and storage.

412278-02-5

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412278-02-5 Usage

Uses

Used in Pharmaceutical Industry:
Tert-Butyl 3-hydroxy-3-Methylpyrrolidine-1-carboxylate is used as a synthetic intermediate for the production of various pharmaceutical compounds. Its unique molecular structure allows for the creation of complex molecules with potential therapeutic applications.
Used in Chemical Research:
Tert-Butyl 3-hydroxy-3-Methylpyrrolidine-1-carboxylate is used as a research compound in the field of organic chemistry. Its properties and reactivity are studied to understand its potential applications and to develop new synthetic pathways for the production of other compounds.
Used in Material Science:
Tert-Butyl 3-hydroxy-3-Methylpyrrolidine-1-carboxylate is used as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with unique characteristics, such as improved stability or enhanced reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 412278-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,2,7 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 412278-02:
(8*4)+(7*1)+(6*2)+(5*2)+(4*7)+(3*8)+(2*0)+(1*2)=115
115 % 10 = 5
So 412278-02-5 is a valid CAS Registry Number.

412278-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-hydroxy-3-methylpyrrolidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 3-hydroxy-3-methyl-pyrrolidine-1-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:412278-02-5 SDS

412278-02-5Relevant academic research and scientific papers

BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS THERAPEUTIC AGENTS

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Page/Page column 420-421, (2017/12/18)

This invention is directed to benzenesulfonamide compounds, as stereoisomers, enantiomers, tautomers thereof or mixtures thereof; or pharmaceutically acceptable salts, solvates or prodrugs thereof, for the treatment of diseases or conditions associated with voltage-gated sodium channels, such as epilepsy.

DOPAMINE D2 RECEPTOR LIGANDS

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Page/Page column 151, (2016/07/05)

The present invention relates to novel dopamine D2 receptor ligands. The invention further relates to functionally-biased dopamine D2 receptor ligands and the use of these compounds for treating or preventing central nervous system and systemic disorders associated with dysregulation of dopaminergic activity. The present invention relates to novel compounds that modulate dopamine D2 receptors. In particular, compounds of the present invention show functional selectivity at the dopamine D2 receptors and exhibit selectivity downstream of the D2 receptors, on the 0- arrestin pathway and/or on the cAMP pathway.

Oxalates as Activating Groups for Alcohols in Visible Light Photoredox Catalysis: Formation of Quaternary Centers by Redox-Neutral Fragment Coupling

Nawrat, Christopher C.,Jamison, Christopher R.,Slutskyy, Yuriy,MacMillan, David W. C.,Overman, Larry E.

supporting information, p. 11270 - 11273 (2015/09/21)

Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible light photoredox conditions. Using these precursors, the first net redox-neutral coupling of tertiary and secondary alcohols with electron-deficient alkenes is achieved.

RORγ MODULATORS

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Page/Page column 87, (2015/03/28)

Described are RORγ modulators of the formula (I), or pharmaceutically acceptable salts thereof, wherein all substituents are defined herein. The invention includes stereoisomeric forms of the compounds of formula I, including stereoisomerically-pure, scalemic and racemic form, as well as tautomers thereof. Also provided are pharmaceutical compositions comprising the same. Such compounds and compositions are useful in methods for modulating RORγ activity in a cell and methods for treating a subject suffering from a disease or disorder in which the subject would therapeutically benefit from modulation of RORγ activity, for example, autoimmune and/or inflammatory disorders.

1,4-dihydropyridine-3,5-dicarboxylate Derivatives And Preparation And Use Thereof

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Paragraph 0134; 0135; 0199; 0200, (2014/03/21)

The present invention relates to a 1,4-dihydropyridine-3,5-dicarboxylate compound of general compound (I), a process for preparing the same, a use thereof for the manufacture of a medicament for treating and/or preventing kidney injury, cardiovascular diseases and/or endocrine diseases, as well as a pharmaceutical composition and a pharmaceutical formulation containing said compounds, wherein the definitions of R1, R2, R3, R4, R5, R6, R7, R8, m, n1, n2, p and q are the same as those defined in the description.

1,4-DIHYDROPYRIDINE -3,5-DICARBOXYLATE DERIVATIVES, PREPARATION METHODS AND USES THEREOF

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Paragraph 0119; 0120, (2014/03/25)

The present invention relates to a 1,4-dihydropyridine-3,5-dicarboxylate compound of general compound (I), a process for preparing the same, a use thereof for the manufacture of a medicament for treating and/or preventing kidney injury, cardiovascular diseases and/or endocrine diseases, as well as a pharmaceutical composition and a pharmaceutical formulation containing said compounds, wherein the definitions of R1, R2, R3, R4, R5, R6, R7, R8, m, n1, n2, p and q are the same as those defined in the description.

Antibacterial Compounds

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Paragraph 0514, (2013/10/07)

The present invention provides a compound of the following formula, salts, racemates, diastereomers, enantiomers, esters, carbamates, phosphates, sulfates, deuterated forms and prodrugs thereof. Also provided is the use of these compounds as antibacterials, compositions comprising them and processes for their manufacture.

AZA-BENZOFURANYL COMPOUNDS AND METHODS OF USE

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Page/Page column 123, (2008/06/13)

The invention relates to azabenzofuranyl compounds of Formula (I) with anti-cancer and/or anti-inflammatory activity and more specifically to azabenzofuranyl compounds which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.

THERAPEUTIC AGENTS

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Page/Page column 29, (2010/11/25)

Compounds of formula (I), processes for preparing such compounds, their use in the treatment of obesity, psychiatric disorders, cognitive disorders, memory disorders, schizophrenia, epilepsy, and related conditions, and neurological disorders such as dementia, multiple sclerosis, Parkinson's disease, Huntington's chorea and Alzheimer's disease and pain related disorders and to pharmaceutical compositions containing them.

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